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Deroximel DR 231 mg

Renata PLC · Capsule (Enteric Coated)

Generic

Diroximel Fumarate

Strength231 mg
Total Strip5
Strip Size6
Unit Price
200

/ Piece

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Medicine Description

Detailed scientific information regarding the indications, dosage, potential side effects, and guidelines for use during pregnancy of Deroximel DR or the Diroximel Fumarate group is provided below. Always consult a specialist physician before taking any medication.

Deroximel DR 231 mg | INDICATIONS AND USES

Diroximel Fumarate is indicated for the treatment of relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults.


Deroximel DR 231 mg | PHARMACOLOGY

The mechanism by which diroximel fumarate exerts its therapeutic effect in multiple sclerosis is unknown. MMF, the active metabolite of diroximel fumarate, has been shown to activate the nuclear factor (erythroid-derived 2)-like 2 (Nrf2) pathway in vitro and in vivo in animals and humans. The Nrf2 pathway is involved in the cellular response to oxidative stress. MMF has been identified as a nicotinic acid receptor agonist in vitro.


Deroximel DR 231 mg | DOSAGE & ADMINISTRATION

Blood Tests Prior to Initiation of Diroximel: Obtain the following prior to treatment with Diroximel:

A complete blood cell count (CBC), including lymphocyte count
Serum aminotransferase, alkaline phosphatase, and total bilirubin levels

Dosing Information: The starting dosage for Diroximel is 231 mg twice a day orally. After 7 days, the dosage should be increased to the maintenance dosage of 462 mg (administered as two 231 mg capsules) twice a day orally. Temporary dosage reductions to 231 mg twice a day may be considered for individuals who do not tolerate the maintenance dosage. Within 4 weeks, the recommended dosage of 462 mg twice a day should be resumed. Discontinuation of Diroximel should be considered for patients unable to tolerate return to the maintenance dosage. Administration of non-enteric coated aspirin (up to a dose of 325 mg) 30 minutes prior to Diroximel dosing may reduce the incidence or severity of flushing.Administration Instructions: Swallow Diroximel capsules whole and intact. Do not crush or chew, or sprinkle the capsule contents on food. If taken with food, avoid a high-fat, high-calorie meal/snack; the meal/snack should contain no more than 700 calories and no more than 30 g fat.


Deroximel DR 231 mg | SIDE EFFECTS

The following important adverse reactions are shown:

Anaphylaxis and Angioedema
Progressive Multifocal Leukoencephalopathy
Herpes Zoster and Other Serious Opportunistic Infections
Lymphopenia
Liver Injury
Flushing


Deroximel DR 231 mg | USE DURING PREGNANCY AND LACTATION

There are no adequate data on the developmental risk associated with the use of Diroximel or dimethyl fumarate (which has the same active metabolite as Diroximel) in pregnant women. There are no data on the presence of diroximel fumarate or metabolites (MMF, HES) in human milk. The effects on the breastfed infant and on milk production are unknown.


Deroximel DR 231 mg | PRECAUTIONS & WARNINGS

Anaphylaxis and Angioedema: Discontinue and do not restart diroximel if these occur.Progressive Multifocal Leukoencephalopathy (PML): Withhold diroximel at the first sign or symptom suggestive of PML.Herpes zoster and other serious opportunistic infections: Consider withholding diroximel in cases of serious infection until the infection has resolved.Lymphopenia: Obtain a CBC including lymphocyte count before initiating diroximel, after 6 months, and every 6 to 12 months thereafter. Consider interruption of diroximel if lymphocyte counts <0.5 × 109/L persist for more than six months.Liver Injury: Obtain serum aminotransferase, alkaline phosphatase, and total bilirubin levels before initiating diroximel and during treatment, as clinically indicated. Discontinue diroximel if clinically significant liver injury induced by diroximel is suspected.


Deroximel DR 231 mg | USE IN SPECIAL POPULATIONS

Pediatric Use: Safety and effectiveness in pediatric patients have not been established.Geriatric Use: Clinical studies of Dimethyl fumarate and Diroximel did not include sufficient numbers of patients aged 65 years and over to determine whether they respond differently from younger patients.Renal Impairment: No dosage adjustment is necessary in patients with mild renal impairment.


Deroximel DR 231 mg | STORAGE CONDITIONS

Keep below 30°C temperature, away from light & moisture. Keep out of the reach of children.

⚠ Disclaimer

The information provided on All Samadhan is intended for general informational purposes only and is prepared based on our best practices. It is not a substitute for professional medical advice, diagnosis, or treatment. While we strive to keep the information accurate and up to date, we do not guarantee its completeness or accuracy. The absence of specific information or warnings about any medicine or service should not be considered as an assurance or endorsement by All Samadhan. All Samadhan shall not be held responsible for any consequences arising from the use of this information. We strongly recommend consulting a qualified healthcare professional or physician for any medical concerns, questions, or clarifications.All Samadhan is a digital healthcare software platform operated by MS Genius Experts. We provide technology solutions for pharmacies and healthcare providers; we are not a direct seller or dispenser of prescription medicines

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N:B-All Samadhan is a digital healthcare software platform operated by MS Genius Experts. We provide technology solutions for pharmacies and healthcare providers; we are not a direct seller or dispenser of prescription medicines"

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